Interpretation of lung function tests in the sickle-cell haemoglobinopathies.
AUTOR(ES)
Miller, G J
RESUMO
Prediction equations have been evolved for the assessment of vital capacity, total lung capacity, and the single breath carbon monoxide transfer factor in haemoglobin SS and haemoglobin SC disease. These relationships take account of the growth disorder and anaemia in the sickle-cell states. The results suggest that, in the clinically stable state, any effects of alveolar capillary sickling and haemoconcentration and any altered reactivity of haemoglobins S and C with the test gas are of no significance for clinical respiratory physiology. Sex differences in lung function appear independent of haemoglobin type.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=470851Documentos Relacionados
- Open-heart surgery in sickle-cell haemoglobinopathies: report of 15 cases
- A rapid whole blood solubility test to differentiate the sickle-cell trait from sickle-cell anaemia
- The Inheritance of Sickle-Cell Anaemia in Man
- Bronchopulmonary anastomoses in sickle-cell anaemia
- Coagulation fibrinolysis in sickle-cell disease